5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile

Product Name: 5-(2-fluorophenyl)-1H-pyrrole-3-carbonitrile

CAS: 1240948-77-9

MF: C11H7FN2

MW: 186.19

Boiling Point: 364.7±32.0 °C(Predicted)

Density: 1.28±0.1 g/cm3(Predicted)

storage temp: Sealed in dry,Room Temperature

Solubility: NA

Form: Solid

Pka: 13.87±0.50(Predicted)

Color: NA

InChI: InChI=1S/C11H7FN2/c12-10-4-2-1-3-9(10)11-5-8(6-13)7-14-11/h1-5,7,14H

InChIKey: ZDEFHFJZEDEKJO-UHFFFAOYSA-N

SMILES: N1C(C2=CC=CC=C2F)=CC(C#N)=C1

Here are some descriptions of the properties of this compound:

1. Appearance: 5-(2-fluorophenyl)-1H-pyrrole-3-carrotonitrile may be a solid crystal with certain crystallinity.

2. Solubility: The compound has low solubility in water and can be dissolved in organic solvents (such as ethanol, dimethylformamide, etc.).

4. Chemical reaction: There is a fluorine atom on the benzene ring in the compound, which makes the compound have a certain chemical activity. It can perform electrophilic addition reactions, nucleophilic addition reactions, and other reaction types.

5-(2-fluorophenyl)-1H-pyrrole-3-carbotonitrile is an organic compound with a wide range of applications and synthesis methods.

One of its main applications is as an important intermediate in organic synthesis. Specifically, this compound is an important aromatic compound derivative.

Secondly, 5-(2-fluorophenyl)-1H-pyrrole-3-carrotonitrile can also be used as a research object in materials science. It has certain optoelectronic properties and has certain application potential in the field of optoelectronic devices. This compound has good conductivity and light absorption properties, which is of great significance for the preparation and performance control of organic optoelectronic devices.

Synthesis method, the synthesis of 5-(2-fluorophenyl)-1H-pyrrole-3-carrotonitrile can usually be carried out by the following steps:

Start with the pyrrole initiation compound. Pyrrole can be synthesized by a variety of methods, such as by the reaction of bromide and amine to obtain the pyrrole ring.

Cyano is introduced on the pyrrole ring. This can be done by converting an existing functional group to a cyano group, or by introducing the cyano group through a nucleophilic substitution reaction.

Fluorophenyl groups are introduced on the pyrrole ring. This can be done by a nucleophilic substitution reaction that introduces a fluorophenyl group onto the pyrrole.

There are also a variety of methods to synthesize this compound, which can be selected according to specific needs.